DE20106651U1 - Hair Dye - Google Patents
Hair DyeInfo
- Publication number
- DE20106651U1 DE20106651U1 DE20106651U DE20106651U DE20106651U1 DE 20106651 U1 DE20106651 U1 DE 20106651U1 DE 20106651 U DE20106651 U DE 20106651U DE 20106651 U DE20106651 U DE 20106651U DE 20106651 U1 DE20106651 U1 DE 20106651U1
- Authority
- DE
- Germany
- Prior art keywords
- amino
- dihydroxynaphthalene
- diamino
- diaminopyrazole
- hydroxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 18
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 230000003647 oxidation Effects 0.000 claims description 10
- 238000007254 oxidation reaction Methods 0.000 claims description 10
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 8
- 229940120503 dihydroxyacetone Drugs 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 6
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 5
- 210000004209 hair Anatomy 0.000 claims description 4
- 239000002243 precursor Substances 0.000 claims description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 4
- MUYIVZJCWVZYHR-UHFFFAOYSA-N 4,5-diamino-1,2-dihydropyrazol-3-one Chemical compound NC=1NNC(=O)C=1N MUYIVZJCWVZYHR-UHFFFAOYSA-N 0.000 claims description 3
- QZBGOTVBHYKUDS-UHFFFAOYSA-N 5-amino-1,2-dihydropyrazol-3-one Chemical compound NC1=CC(=O)NN1 QZBGOTVBHYKUDS-UHFFFAOYSA-N 0.000 claims description 3
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 claims description 3
- KZQYIMCESJLPQH-UHFFFAOYSA-N Demethylated antipyrine Chemical compound N1C(C)=CC(=O)N1C1=CC=CC=C1 KZQYIMCESJLPQH-UHFFFAOYSA-N 0.000 claims description 3
- 150000003852 triazoles Chemical class 0.000 claims description 3
- OBENDWOJIFFDLZ-UHFFFAOYSA-N (3,5-dimethylpyrazol-1-yl)methanol Chemical compound CC=1C=C(C)N(CO)N=1 OBENDWOJIFFDLZ-UHFFFAOYSA-N 0.000 claims description 2
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 2
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 claims description 2
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims description 2
- PZKPUGIOJKNRQZ-UHFFFAOYSA-N 1-methylcyclohexa-3,5-diene-1,3-diamine Chemical compound CC1(N)CC(N)=CC=C1 PZKPUGIOJKNRQZ-UHFFFAOYSA-N 0.000 claims description 2
- KGBBJPZIDRELDP-UHFFFAOYSA-N 1h-pyrazole-3,5-diamine Chemical compound NC=1C=C(N)NN=1 KGBBJPZIDRELDP-UHFFFAOYSA-N 0.000 claims description 2
- SWFNPENEBHAHEB-UHFFFAOYSA-N 2-amino-4-chlorophenol Chemical compound NC1=CC(Cl)=CC=C1O SWFNPENEBHAHEB-UHFFFAOYSA-N 0.000 claims description 2
- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 claims description 2
- BMTSZVZQNMNPCT-UHFFFAOYSA-N 2-aminopyridin-3-ol Chemical compound NC1=NC=CC=C1O BMTSZVZQNMNPCT-UHFFFAOYSA-N 0.000 claims description 2
- XWPOHTNPKCQUNJ-UHFFFAOYSA-N 2-methyl-1-phenyl-3h-pyrazole Chemical compound CN1CC=CN1C1=CC=CC=C1 XWPOHTNPKCQUNJ-UHFFFAOYSA-N 0.000 claims description 2
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 claims description 2
- SRJCJJKWVSSELL-UHFFFAOYSA-N 2-methylnaphthalen-1-ol Chemical compound C1=CC=CC2=C(O)C(C)=CC=C21 SRJCJJKWVSSELL-UHFFFAOYSA-N 0.000 claims description 2
- OBOSXEWFRARQPU-UHFFFAOYSA-N 2-n,2-n-dimethylpyridine-2,5-diamine Chemical compound CN(C)C1=CC=C(N)C=N1 OBOSXEWFRARQPU-UHFFFAOYSA-N 0.000 claims description 2
- IBVXVTTWHOHJNF-UHFFFAOYSA-N 3,5-diaminopyrazole-1-carboxamide Chemical compound NC(=O)N1N=C(N)C=C1N IBVXVTTWHOHJNF-UHFFFAOYSA-N 0.000 claims description 2
- SDXAWLJRERMRKF-UHFFFAOYSA-N 3,5-dimethyl-1h-pyrazole Chemical compound CC=1C=C(C)NN=1 SDXAWLJRERMRKF-UHFFFAOYSA-N 0.000 claims description 2
- MESJRHHDBDCQTH-UHFFFAOYSA-N 3-(dimethylamino)phenol Chemical compound CN(C)C1=CC=CC(O)=C1 MESJRHHDBDCQTH-UHFFFAOYSA-N 0.000 claims description 2
- NCUABBHFJSFKOJ-UHFFFAOYSA-N 3-amino-5-methylphenol Chemical compound CC1=CC(N)=CC(O)=C1 NCUABBHFJSFKOJ-UHFFFAOYSA-N 0.000 claims description 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 2
- 229940018563 3-aminophenol Drugs 0.000 claims description 2
- GRLQBYQELUWBIO-UHFFFAOYSA-N 4,6-dichlorobenzene-1,3-diol Chemical compound OC1=CC(O)=C(Cl)C=C1Cl GRLQBYQELUWBIO-UHFFFAOYSA-N 0.000 claims description 2
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims description 2
- MUHQJMUYRYHUIW-UHFFFAOYSA-N 5-amino-4-methoxy-2-methylphenol Chemical compound COC1=CC(C)=C(O)C=C1N MUHQJMUYRYHUIW-UHFFFAOYSA-N 0.000 claims description 2
- BGSKARBUPDZLFR-UHFFFAOYSA-N 6-hydroxy-3,5-dimethoxy-1h-pyridin-2-one Chemical compound COC1=CC(OC)=C(O)N=C1O BGSKARBUPDZLFR-UHFFFAOYSA-N 0.000 claims description 2
- LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Chemical compound OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 claims description 2
- 230000008878 coupling Effects 0.000 claims description 2
- 238000010168 coupling process Methods 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 238000004043 dyeing Methods 0.000 claims description 2
- PKWIYNIDEDLDCJ-UHFFFAOYSA-N guanazole Chemical compound NC1=NNC(N)=N1 PKWIYNIDEDLDCJ-UHFFFAOYSA-N 0.000 claims description 2
- FZZQNEVOYIYFPF-UHFFFAOYSA-N naphthalene-1,6-diol Chemical compound OC1=CC=CC2=CC(O)=CC=C21 FZZQNEVOYIYFPF-UHFFFAOYSA-N 0.000 claims description 2
- ZUVBIBLYOCVYJU-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21 ZUVBIBLYOCVYJU-UHFFFAOYSA-N 0.000 claims description 2
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 claims description 2
- PIDZGPMVKVVCGG-UHFFFAOYSA-N 1-(3,4-diamino-1h-pyrazol-5-yl)ethanol Chemical compound CC(O)C1=NNC(N)=C1N PIDZGPMVKVVCGG-UHFFFAOYSA-N 0.000 claims 1
- BLQFHJKRTDIZLX-UHFFFAOYSA-N 5-amino-2-methoxyphenol Chemical compound COC1=CC=C(N)C=C1O BLQFHJKRTDIZLX-UHFFFAOYSA-N 0.000 claims 1
- ATCBPVDYYNJHSG-UHFFFAOYSA-N 6-methoxy-2-n-methylpyridine-2,3-diamine Chemical compound CNC1=NC(OC)=CC=C1N ATCBPVDYYNJHSG-UHFFFAOYSA-N 0.000 claims 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 239000000118 hair dye Substances 0.000 description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 8
- 229910052802 copper Inorganic materials 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- 239000007800 oxidant agent Substances 0.000 description 6
- 150000002978 peroxides Chemical class 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 244000309464 bull Species 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- MJAVQHPPPBDYAN-UHFFFAOYSA-N 2,6-dimethylbenzene-1,4-diamine Chemical compound CC1=CC(N)=CC(C)=C1N MJAVQHPPPBDYAN-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- JSYBAZQQYCNZJE-UHFFFAOYSA-N benzene-1,2,4-triamine Chemical compound NC1=CC=C(N)C(N)=C1 JSYBAZQQYCNZJE-UHFFFAOYSA-N 0.000 description 2
- 239000012458 free base Substances 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 235000013772 propylene glycol Nutrition 0.000 description 2
- 150000003217 pyrazoles Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- NKNCGBHPGCHYCQ-UHFFFAOYSA-N (2,5-diaminophenyl)methanol Chemical compound NC1=CC=C(N)C(CO)=C1 NKNCGBHPGCHYCQ-UHFFFAOYSA-N 0.000 description 1
- PQWHYMIYFPATGG-UHFFFAOYSA-N (4-amino-5-oxo-1,2-dihydropyrazol-3-yl)azanium;hydrogen sulfate Chemical compound OS(O)(=O)=O.NC=1NNC(=O)C=1N PQWHYMIYFPATGG-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- DBIJZEYNEPBLGA-UHFFFAOYSA-N 2,4-diamino-3-chlorophenol Chemical compound NC1=CC=C(O)C(N)=C1Cl DBIJZEYNEPBLGA-UHFFFAOYSA-N 0.000 description 1
- HWSJQFCTYLBBOF-UHFFFAOYSA-N 2,5-diamino-4-hydroxy-1h-pyrimidin-6-one Chemical class NC1=NC(O)=C(N)C(O)=N1 HWSJQFCTYLBBOF-UHFFFAOYSA-N 0.000 description 1
- BAYXOGMUGKSOIY-UHFFFAOYSA-N 2,5-diamino-4-methylphenol Chemical compound CC1=CC(N)=C(O)C=C1N BAYXOGMUGKSOIY-UHFFFAOYSA-N 0.000 description 1
- 229940075142 2,5-diaminotoluene Drugs 0.000 description 1
- KZTWOUOZKZQDMN-UHFFFAOYSA-N 2,5-diaminotoluene sulfate Chemical compound OS(O)(=O)=O.CC1=CC(N)=CC=C1N KZTWOUOZKZQDMN-UHFFFAOYSA-N 0.000 description 1
- KWSVXCAQFTWTEF-UHFFFAOYSA-N 2-(2,5-diaminophenyl)ethanol Chemical compound NC1=CC=C(N)C(CCO)=C1 KWSVXCAQFTWTEF-UHFFFAOYSA-N 0.000 description 1
- JGAGLKQYRXRYGP-UHFFFAOYSA-N 2-(3,4-diamino-1h-pyrazol-5-yl)ethanol;sulfuric acid Chemical compound OS(O)(=O)=O.NC=1NN=C(CCO)C=1N JGAGLKQYRXRYGP-UHFFFAOYSA-N 0.000 description 1
- IBCDZZHMNXXYAP-UHFFFAOYSA-N 2-(4,5-diaminopyrazol-1-yl)ethanol;sulfuric acid Chemical compound OS(O)(=O)=O.NC=1C=NN(CCO)C=1N IBCDZZHMNXXYAP-UHFFFAOYSA-N 0.000 description 1
- JLEBZTSKNDQWIO-UHFFFAOYSA-N 2-(4-amino-2-methylanilino)ethanol Chemical compound CC1=CC(N)=CC=C1NCCO JLEBZTSKNDQWIO-UHFFFAOYSA-N 0.000 description 1
- VLZVIIYRNMWPSN-UHFFFAOYSA-N 2-Amino-4-nitrophenol Chemical compound NC1=CC([N+]([O-])=O)=CC=C1O VLZVIIYRNMWPSN-UHFFFAOYSA-N 0.000 description 1
- ISCYHXYLVTWDJT-UHFFFAOYSA-N 2-[4-amino-n-(2-hydroxyethyl)anilino]ethanol Chemical compound NC1=CC=C(N(CCO)CCO)C=C1 ISCYHXYLVTWDJT-UHFFFAOYSA-N 0.000 description 1
- MGLZGLAFFOMWPB-UHFFFAOYSA-N 2-chloro-1,4-phenylenediamine Chemical compound NC1=CC=C(N)C(Cl)=C1 MGLZGLAFFOMWPB-UHFFFAOYSA-N 0.000 description 1
- ZSIMBMYNZHSZGJ-UHFFFAOYSA-N 2-ethylbenzene-1,4-diamine Chemical compound CCC1=CC(N)=CC=C1N ZSIMBMYNZHSZGJ-UHFFFAOYSA-N 0.000 description 1
- HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 description 1
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 description 1
- WTLVAFTZNBFKTI-UHFFFAOYSA-N 2-methylbenzene-1,4-diamine;4-methylcyclohexa-1,5-diene-1,4-diamine Chemical compound CC1=CC(N)=CC=C1N.CC1(N)CC=C(N)C=C1 WTLVAFTZNBFKTI-UHFFFAOYSA-N 0.000 description 1
- DJKXYDZAXRFXCF-UHFFFAOYSA-N 4-(2-aminopropan-2-yl)aniline Chemical compound CC(C)(N)C1=CC=C(N)C=C1 DJKXYDZAXRFXCF-UHFFFAOYSA-N 0.000 description 1
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 description 1
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 1
- HKGOSYWNUBEMMH-UHFFFAOYSA-N 4-n-ethyl-4-n-propan-2-ylbenzene-1,4-diamine Chemical compound CCN(C(C)C)C1=CC=C(N)C=C1 HKGOSYWNUBEMMH-UHFFFAOYSA-N 0.000 description 1
- TWLMSPNQBKSXOP-UHFFFAOYSA-N 6358-09-4 Chemical compound NC1=CC([N+]([O-])=O)=CC(Cl)=C1O TWLMSPNQBKSXOP-UHFFFAOYSA-N 0.000 description 1
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 description 1
- BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- PAPRMXKGBBURHQ-UHFFFAOYSA-M [Na+].CCCCCCCCCCCCOS([O-])(=O)=O.CCCCCCCCC=C/CCCCCCCC(O)=O Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O.CCCCCCCCC=C/CCCCCCCC(O)=O PAPRMXKGBBURHQ-UHFFFAOYSA-M 0.000 description 1
- -1 a-naphthol Chemical compound 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- BXCPYILIGVODMY-UHFFFAOYSA-N anisole;sulfuric acid Chemical compound OS(O)(=O)=O.COC1=CC=CC=C1 BXCPYILIGVODMY-UHFFFAOYSA-N 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- WRPSKOREVDHZHP-UHFFFAOYSA-N benzene-1,4-diamine Chemical compound NC1=CC=C(N)C=C1.NC1=CC=C(N)C=C1 WRPSKOREVDHZHP-UHFFFAOYSA-N 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- KDNFLUWYIMPBSA-UHFFFAOYSA-N hydrogen peroxide;1,3,5-triazine-2,4,6-triamine Chemical compound OO.NC1=NC(N)=NC(N)=N1 KDNFLUWYIMPBSA-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 description 1
- 229960004963 mesalazine Drugs 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000001005 nitro dye Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 229940101267 panthenol Drugs 0.000 description 1
- 235000020957 pantothenol Nutrition 0.000 description 1
- 239000011619 pantothenol Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000001024 permanent hair color Substances 0.000 description 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229960003288 sulfaethidole Drugs 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/496—Triazoles or their condensed derivatives, e.g. benzotriazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Description
' ' ' \.1"&ngr; * : ! &iacgr; A-21/01-U''' \. 1 " ν * : ! &iacgr; A-21/01-U
Die vorliegende Erfindung betrifft ein Haarfärbemittel auf Basis eines mit Peroxid reagierenden Oxidationsfarbstoff-Systems, das dauerhafte intensive Farbtöne liefert, die entweder als solche angewandt werden, oder, in Kombination mit weiteren Entwickler- und/oder Kupplersubstanzen, zur Erzielung weiterer Farbnuancen benutzt werden können.The present invention relates to a hair dye based on a peroxide-reacting oxidation dye system which provides permanent, intense shades which can either be used as such or, in combination with other developers and/or couplers, to achieve further color nuances.
Die nach wie vor in Haarfärbemitteln meist eingesetzten Entwicklersubstanzen sind 1,4-Diaminobenzol (p-Phenylendiamin) und 1-Methyl-2,5-diaminobenzol (p-Toluylendiamin). Die Verwendung dieser Substanzen wird den farbtechnischen WünschenThe developer substances most commonly used in hair dyes are 1,4-diaminobenzene (p-phenylenediamine) and 1-methyl-2,5-diaminobenzene (p-toluenediamine). The use of these substances is based on the color-technical requirements
K.K.
der Anwender zwar weitgehend gerecht, es gibt jedoch immer noch Farbnuancen, die dadurch nicht voll erreicht bzw. noch intensiviert werden können.Although the user's needs are largely met, there are still color nuances that cannot be fully achieved or intensified.
Es wurde auch bereits vorgeschlagen, diese Lücke durch Verwendung alternativer Entwicklersubstanzen zu schließen. Dies ist in beschränktem Umfang möglich durch den Einsatz von 2-(2,5-Diaminophenyl)ethanol (vgl. EP-A 7537 und EP-B 400 330); jedoch müssen dann Abstriche in der Farbintensität anderer Nuancen hingenommenIt has already been proposed to close this gap by using alternative developing substances. This is possible to a limited extent by using 2-(2,5-diaminophenyl)ethanol (cf. EP-A 7537 and EP-B 400 330); however, this would mean that the colour intensity of other shades would be reduced.
werden. r become. r
Eine weitere befriedigende Lösung dieses Problems wird auch durch den in der EP-A 615 743 beschriebenen Einsatz von 2-(2'-Hydroxyethylamino)-5-aminotoluol bzw. dessen wasserlöslichen Salzen als Entwicklersubstanzen in Haarfärbemitteln erreicht.A further satisfactory solution to this problem is also achieved by the use of 2-(2'-hydroxyethylamino)-5-aminotoluene or its water-soluble salts as developing substances in hair dyes, as described in EP-A 615 743.
Selbst dadurch bleiben jedoch noch farbtechnische Wünsche offen.Even so, there are still some color-related wishes that remain unfulfilled.
Auch Pyrazol und dessen Derivate wie 3,4-Diamino-5-hydroxypyrazol sind bereits als Bestandteil von Oxidations-Haarfärbemitteln vorgeschlagen worden.
Es war jedoch bisher nicht möglich, damit Färbungen in allen wünschenswerten Farbtönen und vor allem in der wünschenswerten Intensität herzustellen.Pyrazole and its derivatives such as 3,4-diamino-5-hydroxypyrazole have also been suggested as components of oxidative hair dyes.
However, it has not been possible to produce dyes in all desirable shades and, above all, in the desired intensity.
• ··
Die Erfindung geht daher von der Aufgabenstellung aus, ein Haarfärbemittel zu schaffen, das zur Herstellung einer großen Anzahl von Farbtönen geeignet ist und vor allem eine besonders intensive glänzende Färbung bewirkt.The invention is therefore based on the task of creating a hair dye which is suitable for producing a large number of shades and, above all, produces a particularly intense, shiny color.
Diese Aufgabe wird dadurch gelöst, daß ein solches Haarfärbemittel mindestens ein mit Peroxid reagierendes Oxidationsfarbstoff-System enthält, das aus einer Kombination aus mindestens einem Pyrazol bzw. dessen wasserlöslichen Salzen und/oder einem substituierten Triazol und 0,01 bis 10, vorzugsweise 0,05 bis 5 Gew.-% Dihydroxyaceton, berechnet auf die Gesamtmenge des Mittels, in wäßriger Grundlage enthält.This object is achieved in that such a hair dye contains at least one oxidation dye system which reacts with peroxide and which consists of a combination of at least one pyrazole or its water-soluble salts and/or a substituted triazole and 0.01 to 10, preferably 0.05 to 5% by weight of dihydroxyacetone, calculated on the total amount of the agent, in an aqueous base.
Bevorzugte Pyrazole sind dabei Pyrazol selbst sowie die substituierten Pyrazole 1 -HydroxyethyW.S-diaminopyrazol, 3,4-Diamino-5-hydroxypyrazol, 3,5-Diaminopyrazol, 3,5-Diaminopyrazol-i-carboxamid, 3-Amino-5-hydroxypyrazol, 1-Phenyl-2-methylpyrazol, 1-Phenyl-3-methylpyrazol-5-on, 3,5-Dimethylpyrazol, 3,5-Dimethylpyrazol-1-methanol und/oder 3,5-Diamino-1,2,4-thazol bzw. deren wasserlösliche Salze.Preferred pyrazoles are pyrazole itself and the substituted pyrazoles 1-hydroxyethylW.S-diaminopyrazole, 3,4-diamino-5-hydroxypyrazole, 3,5-diaminopyrazole, 3,5-diaminopyrazole-i-carboxamide, 3-amino-5-hydroxypyrazole, 1-phenyl-2-methylpyrazole, 1-phenyl-3-methylpyrazol-5-one, 3,5-dimethylpyrazole, 3,5-dimethylpyrazole-1-methanol and/or 3,5-diamino-1,2,4-ethazole or their water-soluble salts.
Vorzugsweise enthält das erfindungsgemäße Mittel mindestens eine Kupplersubstanz, beispielsweise ausgewählt aus Resorcin, 2-Methylresorcin, 4-Chlorresorcin, 2-Amino-4-chlorphenoli 5-Amino-4-methoxy-2-methylphenol, 2-Aminophenol, 3-Aminophenol, 1-Methyl-2-hydroxy-4-aminobenzol, 3-N,N-Dimethylaminophenol, 2,6-Dihydroxy-3,5-dimethoxypyridin, 5-Amino-3-methylphenol, 6-Amino-3-methylphenol, S-Amino^-methylamino-o-methoxypyridin, 2-Amino-3-hydroxypyridin, 2-Dimethylamino-5-aminopyridin, 2,6-Diaminopyhdin, 1,3-Diaminobenzol, 1 -Amino-3-(2'-hydroxyethylamino)benzol, 1 -Amino-3-[bis(2'-hydroxyethyl)amino]benzol, a-Naphthol, 4,6-Dichlorresorcin, 1,3-Diaminotoluol, 1-Hydroxynaphthalin, 4-Hydroxy-1,2-methylendioxybenzol, 1,5-Dihydroxynaphthalin, 1,6-Dihydroxynaphthalin, 1,7-Dihydroxynaphthalin, 2,7-Dihydroxynaphthalin, 1-Hydroxy-2-methylnaphthalin, 4-Hydroxy-1,2-methyldioxybenzol, 2,4-Diamino-3-chlorphenol und/oder 1-Methoxy-2-amino-4-(2'-hydroxyethylamino)benzol bzw. deren wasserlöslichen Salzen.The agent according to the invention preferably contains at least one coupling substance, for example selected from resorcinol, 2-methylresorcinol, 4-chlororesorcinol, 2-amino-4-chlorophenol, 5-amino-4-methoxy-2-methylphenol, 2-aminophenol, 3-aminophenol, 1-methyl-2-hydroxy-4-aminobenzene, 3-N,N-dimethylaminophenol, 2,6-dihydroxy-3,5-dimethoxypyridine, 5-amino-3-methylphenol, 6-amino-3-methylphenol, S-amino^-methylamino-o-methoxypyridine, 2-amino-3-hydroxypyridine, 2-dimethylamino-5-aminopyridine, 2,6-diaminopyridine, 1,3-diaminobenzene, 1-amino-3-(2'-hydroxyethylamino)benzene, 1-amino-3-[bis(2'-hydroxyethyl)amino]benzene, a-naphthol, 4,6-dichlororesorcinol, 1,3-diaminotoluene, 1-hydroxynaphthalene, 4-hydroxy-1,2-methylenedioxybenzene, 1,5-dihydroxynaphthalene, 1,6-dihydroxynaphthalene, 1,7-dihydroxynaphthalene, 2,7-dihydroxynaphthalene, 1-hydroxy-2-methylnaphthalene, 4-hydroxy-1,2-methyldioxybenzene, 2,4-diamino-3-chlorophenol and/or 1-methoxy-2-amino-4-(2'-hydroxyethylamino)benzene or their water-soluble salts.
•••:..: ' L·"·' ·: I 7 A-21/01••• : .. : 'L·"·' ·: I 7 A-21/01
Damit soll jedoch der Zusatz weiterer Entwickler- und Kupplersubstanzen keineswegs ausgeschlossen sein.However, this does not mean that the addition of further developers and couplers should be excluded.
Bei Anwendung dieser Zusammensetzungen auf Basis einer üblichen Grundlage werden nach der Oxidation mit Peroxid sehr ausdrucksvolle, intensive, dauerhafte Haarfärbungen erhalten, die durch Zusatz entsprechender weiterer Entwickler- und Kupplersubstanzen noch zu anderen Farbnuancen variiert werden können.
Auch die zusätzliche Mitverwendung weiterer, an sich bekannter Entwicklersubstanzen ist möglich.When these compositions are used on a conventional base, very expressive, intense, permanent hair colors are obtained after oxidation with peroxide, which can be varied to other color nuances by adding appropriate additional developers and couplers.
The additional use of other known developing substances is also possible.
Als solche sind vorzugsweise 1,4-Diaminobenzol und substituierte p-Phenylendiamine, insbesondere 2,5-Diaminotoluol, 2-n-Propyl- bzw. 2-Ethyl-p-phenylendiamin, 2,6-Dimethyl-p-phenylendiamin, 2-(2,5-Diaminophenylen)ethanol, 1-Amino-4-bis-(2'-hydroxyethyl)aminobenzol, 2-(-2-Hydroxyethylamino)-5-aminotoluol, 4,4'-Diaminodiphenylamin, 4-Aminodiphenylamin, 2-Amino-5-N,N-diethylaminotoluol, 4-Amino-N-ethyl-N-isopropylanilin, 2-Chlor-p-phenylendiamin, 1 ß-Hydroxyethyl-2,5-diamino-4-methylbenzol, 2-Methoxy-p-phenylendiamin, &Ngr;,&Ngr;-Diethyl-p-phenylendiamin, 1 -Amino-4-ß-methoxyethylaminobenzol, 1 -Dimethylamino-4-anninobenzol, 1-Hydroxy-2,5-diamino-4-methylbenzol, 1-Hydroxymethyl-2,5-diaminobenzol, 1,3-Dimethyl-2,5-diaminobenzol, 1,4-Diaminoisopropylbenzol, 1 -Amino-4-ß-hydroxypropylaminobenzol, 2-Aminophenol, 4-Aminophenole und deren Derivate, Tetraaminopyrimidine, Triaminohydroxypyrimidine, Diaminodihydroxypyrimidine, 5-Aminosalicylsäure und/oder 1,2,4-Triaminobenzol bzw. deren wasserlösliche Salze zu erwähnen.As such, preferably 1,4-diaminobenzene and substituted p-phenylenediamines, in particular 2,5-diaminotoluene, 2-n-propyl- or 2-ethyl-p-phenylenediamine, 2,6-dimethyl-p-phenylenediamine, 2-(2,5-diaminophenylene)ethanol, 1-amino-4-bis-(2'-hydroxyethyl)aminobenzene, 2-(-2-hydroxyethylamino)-5-aminotoluene, 4,4'-diaminodiphenylamine, 4-aminodiphenylamine, 2-amino-5-N,N-diethylaminotoluene, 4-amino-N-ethyl-N-isopropylaniline, 2-chloro-p-phenylenediamine, 1 ß-hydroxyethyl-2,5-diamino-4-methylbenzene, 2-methoxy-p-phenylenediamine, &Ngr;,&Ngr;-diethyl-p-phenylenediamine, 1-amino-4-ß-methoxyethylaminobenzene, 1-dimethylamino-4-aminobenzene, 1-hydroxy-2,5-diamino-4-methylbenzene, 1-hydroxymethyl-2,5-diaminobenzene, 1,3-dimethyl-2,5-diaminobenzene, 1,4-diaminoisopropylbenzene, 1-amino-4-ß-hydroxypropylaminobenzene, 2-aminophenol, 4-aminophenols and their derivatives, tetraaminopyrimidines, triaminohydroxypyrimidines, diaminodihydroxypyrimidines, 5-aminosalicylic acid and/or 1,2,4-triaminobenzene or their water-soluble salts.
Die Gesamtkonzentration der Entwicklersubstanzen liegt üblicherweise zwischen etwa 0,05 und 5 %, vorzugsweise 0,1 und 4 %, insbesondere 0,25 bis 0,5 % und 2,5 bis 3 % Gew.-% der Gesamtzusammensetzung des Haarfärbemittels (ohne Oxidationsmittel), wobei sich die Angaben jeweils auf den Anteil an freier Base beziehen.The total concentration of the developing substances is usually between about 0.05 and 5%, preferably 0.1 and 4%, in particular 0.25 to 0.5% and 2.5 to 3% by weight of the total composition of the hair dye (without oxidizing agent), whereby the information in each case refers to the proportion of free base.
Das bevorzugte Gewichtsverhältnis der genannten Entwicklersubstanzen zu den weiteren Entwickler- und Kupplersubstanzen liegt dabei zwischen etwa 1:8 bis 8:1, vorzugsweise etwa:!" 5 bts.5*M ,.fnsbesorfdepeM :'2 bife 2 :M; ·:The preferred weight ratio of the developer substances mentioned to the other developer and coupler substances is between about 1:8 and 8:1, preferably about:!" 5 bts.5*M ,.fnsbesorfdepeM :'2 bife 2 :M; ·:
Die Kupplersubstanz(en) als Reaktionspartner der Entwicklersubstanz(en) liegen in den erfindungsgemäßen Haarfärbemitteln etwa im gleichen molaren Anteil wie die Entwicklersubstanzen vor, d. h., also in Mengen von 0,01 bis 5,0%, vorzugsweise 0,05 bis 4 %, insbesondere 0,1 bis 3 Gew.-% der Gesamtzusammensetzung (ohne Oxidationsmittel), wobei sich die Angaben jeweils auf, den Anteil an freier Base beziehen.The coupler substance(s) as reaction partner of the developer substance(s) are present in the hair dyes according to the invention in approximately the same molar proportion as the developer substances, i.e. in amounts of 0.01 to 5.0%, preferably 0.05 to 4%, in particular 0.1 to 3% by weight of the total composition (without oxidizing agent), whereby the information in each case refers to the proportion of free base.
Der Anteil an Dihydroxyaceton liegt vorzugsweise bei etwa 0,25 bis 2,5, insbesondere bei etwa 0,5 bis 2 Gew.-% des Farbmittels (ohne Oxidationsmittelzusammensetzung). The proportion of dihydroxyacetone is preferably about 0.25 to 2.5, in particular about 0.5 to 2 wt.% of the colorant (without oxidizing agent composition).
Die erfindungsgemäßen Zusammensetzungen können erwünschtenfalls auch sogenannte Nuanceure zur Feineinstellung des gewünschten Farbtones, insbesondere auch direktziehende Farbstoffe, enthalten.If desired, the compositions according to the invention can also contain so-called shading agents for fine-tuning the desired color tone, in particular direct dyes.
Solche Nuanceure sind beispielsweise Nitrofarbstoffe wie 2-Amino-4,6-dinitrophenol, 2-Amino-4-nitrophenol, 2-Amino-6-chlor-4-nitrophenol, etc., vorzugsweise in Mengen von etwa 0,05 bis 2,5%, insbesondere 0,1 bis 1% Gew.-% der Farbzusammensetzung (ohne Oxidationsmittel).Such nuancers are, for example, nitro dyes such as 2-amino-4,6-dinitrophenol, 2-amino-4-nitrophenol, 2-amino-6-chloro-4-nitrophenol, etc., preferably in amounts of about 0.05 to 2.5%, in particular 0.1 to 1% by weight of the color composition (without oxidizing agent).
Die erfindungsgemäßen Haarfärbemittel können die in solchen Mitteln üblichen Grund- und Zusatzstoffe, Konditioniermittel, etc. enthalten, die dem Fachmann aus dem Stand der Technik bekannt und beispielsweise in der Monographie von
K. Schrader, "Grundlagen und Rezepturen der Kosmetika", 2. Aufl. (Hüthig Buch Verlag, Heidelberg, 1989), S. 782 bis 815, beschrieben sind. Sie können als Lösungen, Cremes, Gele oder auch in Form von Aerosol-Präparaten vorliegen; geeignete Trägermaterial-Zusammensetzungen sind aus dem Stand der Technik hinreichend bekannt.The hair dyes according to the invention can contain the basic and additive ingredients, conditioning agents, etc. that are customary in such agents and that are known to the person skilled in the art and are described, for example, in the monograph by
K. Schrader, "Fundamentals and formulations of cosmetics", 2nd edition (Hüthig Buch Verlag, Heidelberg, 1989), pp. 782 to 815. They can be in the form of solutions, creams, gels or in the form of aerosol preparations; suitable carrier material compositions are well known from the state of the art.
Zur Applikation wird das erfindungsgemäße Oxidationsfarbstoff-Vorprodukt mit einem Oxidationsmittel vermischt. Bevorzugtes Oxidationsmittel ist Wasserstoffperoxid, beispielsweise in 2- bis 12-prozentiger Konzentration.
Es können jedoch auch andere Peroxide wie Harnstoffperoxid und Melaminperoxid eingesetzt werden.For application, the oxidation dye precursor according to the invention is mixed with an oxidizing agent. The preferred oxidizing agent is hydrogen peroxide, for example in a concentration of 2 to 12 percent.
However, other peroxides such as urea peroxide and melamine peroxide can also be used.
Alternativ zur Peroxidoxidation kann auch eine Luftoxidation vorgenommen werden, beispielsweise, indem eine ein Oxidationsfarbstoffvorprodukt enthaltende Zusammensetzung als Aerosolschaum auf das Haar aufgebracht und dort für etwa 15 bis 30 Minuten einwirken gelassen wird.As an alternative to peroxide oxidation, air oxidation can also be carried out, for example by applying a composition containing an oxidation dye precursor to the hair as an aerosol foam and leaving it there for about 15 to 30 minutes.
Der pH-Wert des applikationsfertigen Haarfärbemittels, d. h. nach Vermischung mit Peroxid, kann sowohl im schwach sauren, d. h. einem Bereich von 5,5 bis 6,9, im neutralen als auch im alkalischen Bereich, d. h. zwischen pH 7,1 und 11 liegen.The pH value of the ready-to-use hair dye, i.e. after mixing with peroxide, can be in the weakly acidic range, i.e. a range from 5.5 to 6.9, in the neutral range or in the alkaline range, i.e. between pH 7.1 and 11.
Im folgenden werden verschiedene Ausführungsbeispiele zur Erläuterung der
Erfindung gegeben.In the following, various examples are given to explain the
invention given.
Grundlagebasis
Stearylalkohol Kokosfettsäuremonoethanolamid 1,2-Propandiolmono/distearat Kokosfettalkoholpolyglykolether Natriumlaurylsulfat ÖlsäureStearyl alcohol Coconut fatty acid monoethanolamide 1,2-propanediol mono/distearate Coconut fatty alcohol polyglycol ether Sodium lauryl sulfate Oleic acid
1,2-Propandiol Na-EDTA1,2-Propanediol Na-EDTA
Natriumsulfit Eiweißhydrolysat Ascorbinsäure ParfümSodium sulphite Protein hydrolysate Ascorbic acid Perfume
Ammoniak, 25%ig Ammoniumchlorid PanthenolAmmonia, 25% ammonium chloride panthenol
WasserWater
8,0 (Gew.-%) 4,5 1,3 4,0 1,0 2,0 1,5 0,5 1,0 0,5 0,2 0,4 1,0 0,5 0,8 ad 100,008.0 (% by weight) 4.5 1.3 4.0 1.0 2.0 1.5 0.5 1.0 0.5 0.2 0.4 1.0 0.5 0, 8 to 100.00
Die erfindungsgemäßen Oxidationsfarbstoff-Kombinationen wurden, unter entsprechender Verringerung des Wassergehalts, in diese Grundlage eingearbeitet.The oxidation dye combinations according to the invention were incorporated into this base, with a corresponding reduction in the water content.
Die Ausfärbungen erfolgten jeweils an Woll-Läppchen und Strähnen aus gebleichtem Menschenhaar, durch Aufbringen einer 1:1-Mischung aus Farbstoff-Vorprodukt und 6%iger Wasserstoffperoxid-Lösung (pH-Wert der Mischung: 9,8) und zwanzigminütiger Einwirkung bei Zimmertemperatur, folgendem Auswaschen und Trocknen.The dyeing was carried out on wool patches and strands of bleached human hair by applying a 1:1 mixture of dye precursor and 6% hydrogen peroxide solution (pH value of the mixture: 9.8) and leaving it for 20 minutes at room temperature, followed by rinsing and drying.
Es wurden die folgenden Färbungen erzielt:The following colorations were achieved:
-7--7-
I · ·
• · &idigr;• · &idgr;
1.1.
pyrazolsulfatHydroxyethyl-4,5-diamino-
pyrazole sulfate
anisolsulfat ^2-Amino-4-hydroxyethyl-amino-
anisole sulfate ^
Intensives DunkelmagentaIntense dark magenta
Intensives RotkupferIntense red copper
TiefviolettDeep purple
Intensives RotkupferIntense red copper
OrangeweißOrange white
Intensives ViolettIntense violet
BraungrauBrown-grey
Intensives MittelblondIntense medium blonde
RotkupferRed copper
GraubraunGrey-brown
-8--8th-
2.2.
In die beschriebene Grundlage wurde die folgende Oxidationsfarbstoffmischung jeweils mit und ohne 0,5 Gew.-% Dihydroxyaceton eingebracht und der pH-Wert so eingestellt, daß beim Vermischen mit 2%-iger wäßriger H2O2-Lösung im Gewichtsverhältnis 1:1 ein pH-Wert der applikationsfertigen Mischung von 6,8 erreicht wurde.The following oxidation dye mixture was introduced into the described base, each with and without 0.5% by weight of dihydroxyacetone, and the pH was adjusted so that when mixed with 2% aqueous H 2 O 2 solution in a weight ratio of 1:1, a pH of the ready-to-use mixture of 6.8 was achieved.
Die Mischung wurde wiederum jeweils auf Woll-Läppchen und Strähnen aus gebleichtem Menschenhaar aufgebracht, nach 15-minütiger Einwirkung ausgewaschen und getrocknet und die Färbung bewertet.The mixture was then applied to wool patches and strands of bleached human hair, washed out and dried after 15 minutes of exposure, and the color was evaluated.
Es wurde folgendes Ergebnis erzielt:
Zusammensetzung The following result was achieved:
composition
Die erfindungsgemäße Zusammensetzung Nr. 1 erzielt eine glänzende, intensive
Ausfärbung, die derjenigen der Zusammensetzung 1a deutlich überlegen war.The composition No. 1 according to the invention achieves a shiny, intense
Coloration that was significantly superior to that of composition 1a.
Claims (5)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE20106651U DE20106651U1 (en) | 2001-04-18 | 2001-04-18 | Hair Dye |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE20106651U DE20106651U1 (en) | 2001-04-18 | 2001-04-18 | Hair Dye |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE20106651U1 true DE20106651U1 (en) | 2002-08-29 |
Family
ID=7955853
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE20106651U Expired - Lifetime DE20106651U1 (en) | 2001-04-18 | 2001-04-18 | Hair Dye |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE20106651U1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2984115A1 (en) * | 2011-12-20 | 2013-06-21 | Oreal | METHOD FOR COLORING OXIDATION RICH IN BODY AND A METAL CATALYST, DEVICE |
| FR2984146A1 (en) * | 2011-12-20 | 2013-06-21 | Oreal | OXIDATION COLORING COMPOSITION RICH IN FATTY BODIES, METHODS AND APPROPRIATE DEVICE |
-
2001
- 2001-04-18 DE DE20106651U patent/DE20106651U1/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2984115A1 (en) * | 2011-12-20 | 2013-06-21 | Oreal | METHOD FOR COLORING OXIDATION RICH IN BODY AND A METAL CATALYST, DEVICE |
| FR2984146A1 (en) * | 2011-12-20 | 2013-06-21 | Oreal | OXIDATION COLORING COMPOSITION RICH IN FATTY BODIES, METHODS AND APPROPRIATE DEVICE |
| WO2013092482A3 (en) * | 2011-12-20 | 2014-01-16 | L'oreal | Oxidation dye composition rich in fatty substances, processes and suitable device for same |
| WO2013092484A3 (en) * | 2011-12-20 | 2014-01-16 | L'oreal | Oxidation dyeing process using a composition rich in fatty substances and comprising a metal catalyst, and device therefor |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP1250908B1 (en) | Hair dye | |
| EP1250909B1 (en) | Hair dye composition | |
| EP1250910B1 (en) | Hair dye composition | |
| DE20017640U1 (en) | Hair Dye | |
| DE10118894A1 (en) | Use of dihydroxyacetone in hair dye compositions based on oxidation dye precursors | |
| EP1297818A2 (en) | Hair dye | |
| EP1250912B1 (en) | Hair dye composition | |
| EP1250911B1 (en) | Hair dye composition | |
| DE20106651U1 (en) | Hair Dye | |
| DE20115893U1 (en) | Hair dyes containing aminopyridine oxidation dye precursors give more brilliant and intense shades when dihydroxy acetone, alloxan, methyl glyoxal or potassium iodide is present | |
| EP0943319B1 (en) | Hair-dye | |
| DE20115892U1 (en) | Hair dyes containing pyrazole and/or substituted triazine oxidation dye precursors give more brilliant and intense shades when dihydroxy acetone, alloxan, methyl glyoxal or potassium iodide is present | |
| DE19735852C2 (en) | Hair dye | |
| DE20106648U1 (en) | Hair Dye | |
| DE19821535C1 (en) | Oxidation hair dye composition containing specific developer | |
| EP0857479A2 (en) | Oxidative hair dye | |
| DE20106649U1 (en) | Hair Dye | |
| DE20106650U1 (en) | Hair Dye | |
| DE20115891U1 (en) | Oxidative dye precursors for human hair contain a 2- or 4-aminophenol, together with dihydroxyacetone, alloxane, methyl glyoxal and/or potassium iodide | |
| DE19735866C1 (en) | Hair colour based on developer coupler system, giving intense permanent colour | |
| DE20106647U1 (en) | Hair Dye | |
| DE20115884U1 (en) | Oxidative dye precursors for human hair contain 1,4-diaminobenzene or a substituted p-phenylenediamine or their salts, together with dihydroxyacetone, alloxane, methyl glyoxal and/or potassium iodide | |
| EP0897713A2 (en) | Hair-dye | |
| DE29711949U1 (en) | Hair dye | |
| DE20007650U1 (en) | Hair dye |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| R207 | Utility model specification |
Effective date: 20021002 |
|
| R081 | Change of applicant/patentee |
Owner name: KPSS-KAO PROFESSIONAL SALON SERVICES GMBH, DE Free format text: FORMER OWNER: GOLDWELL GMBH, 64297 DARMSTADT, DE Effective date: 20030319 |
|
| R156 | Lapse of ip right after 3 years |
Effective date: 20041103 |